» Articles » PMID: 24651135

Systemic Inflammatory Response Syndrome After Administration of Unmodified T Lymphocytes

Overview
Journal Mol Ther
Publisher Cell Press
Date 2014 Mar 22
PMID 24651135
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

Systemic inflammatory response syndrome (SIRS) is a rare systemic inflammatory response associated with fever, tachycardia, profound hypotension, and respiratory distress, which has been reported in cancer patients receiving T cells genetically modified with chimeric antigen receptors to retarget their specificity to tumor-associated antigens. The syndrome usually occurs following significant in vivo expansion of the infused cells and has been associated with tumor destruction/lysis. Analysis of patient plasma has shown elevated cytokine levels, and resolution of symptoms has been reported after administration of steroids and/or antibodies (such as anti-tumor necrosis factor and anti-interleukin (IL)-6 receptor antibodies) that interfere with cytokine responses.To date, SIRS has not been reported in subjects receiving genetically unmodified T cells with native receptors directed against tumor antigens, in which greater physiological control of T-cell activation and expansion may occur. Here, however, we report a patient with bulky refractory Epstein-Barr virus (EBV)-associated lymphoma, who developed this syndrome 2 weeks after receiving T cells directed against EBV antigens through their native receptors. She was treated with steroids and etanercept, with rapid resolution of symptoms. SIRS may therefore occur even when T cells recognize antigens physiologically through their "wild-type" native receptors and should be acknowledged as a potential complication of this therapy.

Citing Articles

SARS-CoV-2-specific T cell therapy for severe COVID-19: a randomized phase 1/2 trial.

Papadopoulou A, Karavalakis G, Papadopoulou E, Xochelli A, Bousiou Z, Vogiatzoglou A Nat Med. 2023; 29(8):2019-2029.

PMID: 37460756 DOI: 10.1038/s41591-023-02480-8.


Development of off-the-shelf hematopoietic stem cell-engineered invariant natural killer T cells for COVID-19 therapeutic intervention.

Li Y, Dunn Z, Garcia Jr G, Carmona C, Zhou Y, Lee D Stem Cell Res Ther. 2022; 13(1):112.

PMID: 35313965 PMC: 8935266. DOI: 10.1186/s13287-022-02787-2.


Reinforcing the Immunocompromised Host Defense against Fungi: Progress beyond the Current State of the Art.

Karavalakis G, Yannaki E, Papadopoulou A J Fungi (Basel). 2021; 7(6).

PMID: 34204025 PMC: 8228486. DOI: 10.3390/jof7060451.


"Cerberus" T Cells: A Glucocorticoid-Resistant, Multi-Pathogen Specific T Cell Product to Fight Infections in Severely Immunocompromised Patients.

Koukoulias K, Papayanni P, Georgakopoulou A, Alvanou M, Laidou S, Kouimtzidis A Front Immunol. 2021; 11:608701.

PMID: 33537032 PMC: 7848034. DOI: 10.3389/fimmu.2020.608701.


Virus-Specific T Cells: Current and Future Use in Primary Immunodeficiency Disorders.

Harris K, Davila B, Bollard C, Keller M J Allergy Clin Immunol Pract. 2018; 7(3):809-818.

PMID: 30581131 PMC: 6401227. DOI: 10.1016/j.jaip.2018.10.049.


References
1.
Leen A, Bollard C, Mendizabal A, Shpall E, Szabolcs P, Antin J . Multicenter study of banked third-party virus-specific T cells to treat severe viral infections after hematopoietic stem cell transplantation. Blood. 2013; 121(26):5113-23. PMC: 3695359. DOI: 10.1182/blood-2013-02-486324. View

2.
Heslop H, Slobod K, Pule M, Hale G, Rousseau A, Smith C . Long-term outcome of EBV-specific T-cell infusions to prevent or treat EBV-related lymphoproliferative disease in transplant recipients. Blood. 2009; 115(5):925-35. PMC: 2817637. DOI: 10.1182/blood-2009-08-239186. View

3.
Rooney C, Smith C, Ng C, Loftin S, Sixbey J, Gan Y . Infusion of cytotoxic T cells for the prevention and treatment of Epstein-Barr virus-induced lymphoma in allogeneic transplant recipients. Blood. 1998; 92(5):1549-55. View

4.
Brentjens R, Riviere I, Park J, Davila M, Wang X, Stefanski J . Safety and persistence of adoptively transferred autologous CD19-targeted T cells in patients with relapsed or chemotherapy refractory B-cell leukemias. Blood. 2011; 118(18):4817-28. PMC: 3208293. DOI: 10.1182/blood-2011-04-348540. View

5.
Brentjens R, Davila M, Riviere I, Park J, Wang X, Cowell L . CD19-targeted T cells rapidly induce molecular remissions in adults with chemotherapy-refractory acute lymphoblastic leukemia. Sci Transl Med. 2013; 5(177):177ra38. PMC: 3742551. DOI: 10.1126/scitranslmed.3005930. View